References
- Blaschuk O, Burdzy K, Fritz IB. Purification and characterization of a cell-aggregating factor (clusterin), the major glycoprotein in ram rete testis fluid. J Biol Chem 1983;258:7714-20.
- de Silva HV, Stuart WD, Park YB, Mao SJ, Gil CM, Wetterau JR, Busch SJ, Harmony JA. Purification and characterization of apolipoprotein J. J Biol Chem 1990;265:14292-7.
- de Silva HV, Harmony JA, Stuart WD, Gil CM, Robbins J. Apolipoprotein J: structure and tissue distribution. Biochemistry 1990;29:5380-9. https://doi.org/10.1021/bi00474a025
- Danik M, Chabot JG, Mercier C, Benabid AL, Chauvin C, Quirion R, Suh M. Human gliomas and epileptic foci express high levels of a mRNA related to rat testicular sulfated glycoprotein 2, a purported marker of cell death. Proc Natl Acad Sci U S A 1991;88:8577-81. https://doi.org/10.1073/pnas.88.19.8577
- Leger JG, Montpetit ML, Tenniswood MP. Characterization and cloning of androgen-repressed mRNAs from rat ventral prostate. Biochem Biophys Res Commun 1987;147:196-203. https://doi.org/10.1016/S0006-291X(87)80106-7
- Tenniswood MP, Guenette RS, Lakins J, Mooibroek M, Wong P, Welsh JE. Active cell death in hormone-dependent tissues. Cancer Metastasis Rev 1992;11:197-220. https://doi.org/10.1007/BF00048064
- Leskov KS, Klokov DY, Li J, Kinsella TJ, Boothman DA. Synthesis and functional analyses of nuclear clusterin, a cell death protein. J Biol Chem 2003;278:11590-600. https://doi.org/10.1074/jbc.M209233200
- Trougakos IP, Djeu JY, Gonos ES, Boothman DA. Advances and challenges in basic and translational research on clusterin. Cancer Res 2009;69:403-6.
- Yang CR, Leskov K, Hosley-Eberlein K, Criswell T, Pink JJ, Kinsella TJ, Boothman DA. Nuclear clusterin/XIP8, an x-ray-induced Ku70-binding protein that signals cell death. Proc Natl Acad Sci U S A 2000;97:5907-12. https://doi.org/10.1073/pnas.97.11.5907
- Shannan B, Seifert M, Leskov K, Willis J, Boothman D, Tilgen W, Reichrath J. Challenge and promise: roles for clusterin in pathogenesis, progression and therapy of cancer. Cell Death Differ 2006;13:12-9. https://doi.org/10.1038/sj.cdd.4401779
- Zhang H, Kim JK, Edwards CA, Xu Z, Taichman R, Wang CY. Clusterin inhibits apoptosis by interacting with activated Bax. Nat Cell Biol 2005;7:909-15. https://doi.org/10.1038/ncb1291
- Moretti RM, Marelli MM, Mai S, Cariboni A, Scaltriti M, Bettuzzi S, Limonta P. Clusterin isoforms differentially affect growth and motility of prostate cells: possible implications in prostate tumorigenesis. Cancer Res 2007;67:10325-33. https://doi.org/10.1158/0008-5472.CAN-07-0516
- Han BH, DeMattos RB, Dugan LL, Kim-Han JS, Brendza RP, Fryer JD, Kierson M, Cirrito J, Quick K, Harmony JA, Aronow BJ, Holtzman DM. Clusterin contributes to caspase-3-independent brain injury following neonatal hypoxia-ischemia. Nat Med 2001;7:338-43. https://doi.org/10.1038/85487
- Wehrli P, Charnay Y, Vallet P, Zhu G, Harmony J, Aronow B, Tschopp J, Bouras C, Viard-Leveugle I, French LE, Gianna-kopoulos P. Inhibition of post-ischemic brain injury by clusterin overexpression. Nat Med 2001;7:977-9. https://doi.org/10.1038/nm0901-977
- Bettuzzi S, Davalli P, Davoli S, Chayka O, Rizzi F, Belloni L, Pellacani D, Fregni G, Astancolle S, Fassan M, Corti A, Baffa R, Sala A. Genetic inactivation of ApoJ/clusterin: effects on prostate tumourigenesis and metastatic spread. Oncogene 2009;28:4344-52. https://doi.org/10.1038/onc.2009.286
- Pucci S, Bonanno E, Pichiorri F, Angeloni C, Spagnoli LG. Modulation of different clusterin isoforms in human colon tumorigenesis. Oncogene 2004;23:2298-304. https://doi.org/10.1038/sj.onc.1207404
- Trougakos IP, Lourda M, Antonelou MH, Kletsas D, Gorgoulis VG, Papassideri IS, Zou Y, Margaritis LH, Boothman DA, Gonos ES. Intracellular clusterin inhibits mitochondrial apoptosis by suppressing p53-activating stress signals and stabilizing the cytosolic Ku70-Bax protein complex. Clin Cancer Res 2009;15:48-59. https://doi.org/10.1158/1078-0432.CCR-08-1805
- Scaltriti M, Santamaria A, Paciucci R, Bettuzzi S. Intracellular clusterin induces G2-M phase arrest and cell death in PC-3 prostate cancer cells1. Cancer Res 2004;64:6174-82. https://doi.org/10.1158/0008-5472.CAN-04-0920
- Takase O, Minto AW, Puri TS, Cunningham PN, Jacob A, Hayashi M, Quigg RJ. Inhibition of NF-kappaB-dependent BclxL expression by clusterin promotes albumin-induced tubular cell apoptosis. Kidney Int 2008;73:567-77. https://doi.org/10.1038/sj.ki.5002563
- Kim N, Yoo JC, Han JY, Hwang EM, Kim YS, Jeong EY, Sun CH, Yi GS, Roh GS, Kim HJ, Kang SS, Cho GJ, Park JY, Choi WS. Human nuclear clusterin mediates apoptosis by interacting with Bcl-XL through C-terminal coiled coil domain. J Cell Physiol 2011 May 12 [Epub]. http://dx.doi.org/10.1002/jcp.22836.
- Lee DH, Ha JH, Kim Y, Bae KH, Park JY, Choi WS, Yoon HS, Park SG, Park BC, Yi GS, Chi SW. Interaction of a putative BH3 domain of clusterin with anti-apoptotic Bcl-2 family proteins as revealed by NMR spectroscopy. Biochem Biophys Res Commun 2011;408:541-7. https://doi.org/10.1016/j.bbrc.2011.04.054
- Cheng EH, Wei MC, Weiler S, Flavell RA, Mak TW, Lindsten T, Korsmeyer SJ. BCL-2, BCL-X(L) sequester BH3 domain-only molecules preventing BAX- and BAK-mediated mitochondrial apoptosis. Mol Cell 2001;8:705-11. https://doi.org/10.1016/S1097-2765(01)00320-3
- Kuwana T, Mackey MR, Perkins G, Ellisman MH, Latterich M, Schneiter R, Green DR, Newmeyer DD. Bid, Bax, and lipids cooperate to form supramolecular openings in the outer mitochondrial membrane. Cell 2002;111:331-42. https://doi.org/10.1016/S0092-8674(02)01036-X
- Kuwana T, Bouchier-Hayes L, Chipuk JE, Bonzon C, Sullivan BA, Green DR, Newmeyer DD. BH3 domains of BH3-only proteins differentially regulate Bax-mediated mitochondrial membrane permeabilization both directly and indirectly. Mol Cell 2005;17:525-35. https://doi.org/10.1016/j.molcel.2005.02.003
- Willis SN, Fletcher JI, Kaufmann T, van Delft MF, Chen L, Czabotar PE, Ierino H, Lee EF, Fairlie WD, Bouillet P, Strasser A, Kluck RM, Adams JM, Huang DC. Apoptosis initiated when BH3 ligands engage multiple Bcl-2 homologs, not Bax or Bak. Science 2007;315:856-9. https://doi.org/10.1126/science.1133289
- Kim H, Tu HC, Ren D, Takeuchi O, Jeffers JR, Zambetti GP, Hsieh JJ, Cheng EH. Stepwise activation of BAX and BAK by tBID, BIM, and PUMA initiates mitochondrial apoptosis. Mol Cell 2009;36:487-99. https://doi.org/10.1016/j.molcel.2009.09.030
- Kim H, Rafiuddin-Shah M, Tu HC, Jeffers JR, Zambetti GP, Hsieh JJ, Cheng EH. Hierarchical regulation of mitochondriondependent apoptosis by BCL-2 subfamilies. Nat Cell Biol 2006;8:1348-58. https://doi.org/10.1038/ncb1499
- Zong WX, Lindsten T, Ross AJ, MacGregor GR, Thompson CB. BH3-only proteins that bind pro-survival Bcl-2 family members fail to induce apoptosis in the absence of Bax and Bak. Genes Dev 2001;15:1481-6. https://doi.org/10.1101/gad.897601
- Chipuk JE, Moldoveanu T, Llambi F, Parsons MJ, Green DR. The BCL-2 family reunion. Mol Cell 2010;37:299-310. https://doi.org/10.1016/j.molcel.2010.01.025
- Youle RJ, Strasser A. The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol 2008;9:47-59. https://doi.org/10.1038/nrm2308
- Day CL, Smits C, Fan FC, Lee EF, Fairlie WD, Hinds MG. Structure of the BH3 domains from the p53-inducible BH3-only proteins Noxa and Puma in complex with Mcl-1. J Mol Biol 2008;380:958-71. https://doi.org/10.1016/j.jmb.2008.05.071
- Kim N, Han JY, Roh GS, Kim HJ, Kang SS, Cho GJ, Park JY, Choi WS. Nuclear clusterin is associated with neuronal apoptosis in the developing rat brain upon ethanol exposure. Alcohol Clin Exp Res 2011 Jul 18 [Epub]. http://dx.doi.org/10.1111/j.1530-0277.2011.01588.x.
- Essabbani A, Margottin-Goguet F, Chiocchia G. Identification of clusterin domain involved in NF-kappaB pathway regulation. J Biol Chem 2010;285:4273-7. https://doi.org/10.1074/jbc.C109.057133
- O'Sullivan J, Whyte L, Drake J, Tenniswood M. Alterations in the post-translational modification and intracellular trafficking of clusterin in MCF-7 cells during apoptosis. Cell Death Differ 2003;10:914-27. https://doi.org/10.1038/sj.cdd.4401254
- Burkey BF, deSilva HV, Harmony JA. Intracellular processing of apolipoprotein J precursor to the mature heterodimer. J Lipid Res 1991;32:1039-48.
- Charnay Y, Imhof A, Vallet PG, Hakkoum D, Lathuiliere A, Poku N, Aronow B, Kovari E, Bouras C, Giannakopoulos P. Clusterin expression during fetal and postnatal CNS development in mouse. Neuroscience 2008;155:714-24. https://doi.org/10.1016/j.neuroscience.2008.06.022
- Iwata A, Browne KD, Chen XH, Yuguchi T, Smith DH. Traumatic brain injury induces biphasic upregulation of ApoE and ApoJ protein in rats. J Neurosci Res 2005;82:103-14. https://doi.org/10.1002/jnr.20607
- Noh HS, Kim DW, Kang SS, Cho GJ, Choi WS. Ketogenic diet prevents clusterin accumulation induced by kainic acid in the hippocampus of male ICR mice. Brain Res 2005;1042:114-8. https://doi.org/10.1016/j.brainres.2005.01.097
- Schreiber SS, Tocco G, Najm I, Baudry M. Seizure activity causes a rapid increase in sulfated glycoprotein-2 messenger RNA in the adult but not the neonatal rat brain. Neurosci Lett 1993;153:17-20. https://doi.org/10.1016/0304-3940(93)90066-T
- Schrijvers EM, Koudstaal PJ, Hofman A, Breteler MM. Plasma clusterin and the risk of Alzheimer disease. JAMA 2011;305:1322-6. https://doi.org/10.1001/jama.2011.381
- Prikrylova Vranova H, Mares J, Nevrly M, Stejskal D, Zapletalova J, Hlustik P, Kanovsky P. CSF markers of neurodegeneration in Parkinson's disease. J Neural Transm 2010;117:1177-81. https://doi.org/10.1007/s00702-010-0462-z
- Hakkoum D, Imhof A, Vallet PG, Boze H, Moulin G, Charnay Y, Stoppini L, Aronow B, Bouras C, Giannakopoulos P. Clusterin increases post-ischemic damages in organotypic hippocampal slice cultures. J Neurochem 2008;106:1791-803.
- Roebuck TM, Mattson SN, Riley EP. A review of the neuroanatomical findings in children with fetal alcohol syndrome or prenatal exposure to alcohol. Alcohol Clin Exp Res 1998;22:339-44. https://doi.org/10.1111/j.1530-0277.1998.tb03658.x
- Lebel C, Rasmussen C, Wyper K, Walker L, Andrew G, Yager J, Beaulieu C. Brain diffusion abnormalities in children with fetal alcohol spectrum disorder. Alcohol Clin Exp Res 2008;32:1732-40. https://doi.org/10.1111/j.1530-0277.2008.00750.x
- Cahill L, McGaugh JL. Mechanisms of emotional arousal and lasting declarative memory. Trends Neurosci 1998;21:294-9. https://doi.org/10.1016/S0166-2236(97)01214-9
- Wyss JM, Van Groen T. Connections between the retrosplenial cortex and the hippocampal formation in the rat: a review. Hippocampus 1992;2:1-11. https://doi.org/10.1002/hipo.450020102
- Van Groen T, Wyss JM. Connections of the retrosplenial granular b cortex in the rat. J Comp Neurol 2003;463:249-63. https://doi.org/10.1002/cne.10757
- Bear MF, Connors BW, Paradiso MA. Neuroscience: exploring the brain. Philadelphia: Lippincott, Williams & Wilkins; 2007.
- Weinberger DR, Egan MF, Bertolino A, Callicott JH, Mattay VS, Lipska BK, Berman KF, Goldberg TE. Prefrontal neurons and the genetics of schizophrenia. Biol Psychiatry 2001;50:825-44. https://doi.org/10.1016/S0006-3223(01)01252-5
- Young C, Roth KA, Klocke BJ, West T, Holtzman DM, Labruyere J, Qin YQ, Dikranian K, Olney JW. Role of caspase-3 in ethanolinduced developmental neurodegeneration. Neurobiol Dis 2005;20:608-14. https://doi.org/10.1016/j.nbd.2005.04.014
- Ke Z, Wang X, Liu Y, Fan Z, Chen G, Xu M, Bower KA, Frank JA, Li M, Fang S, Shi X, Luo J. Ethanol induces endoplasmic reticulum stress in the developing brain. Alcohol Clin Exp Res 2011;35:1574-83.
- Suk K. Microglial signal transduction as a target of alcohol action in the brain. Curr Neurovasc Res 2007;4:131-42. https://doi.org/10.2174/156720207780637261
- Norman AL, Crocker N, Mattson SN, Riley EP. Neuroimaging and fetal alcohol spectrum disorders. Dev Disabil Res Rev 2009;15:209-17. https://doi.org/10.1002/ddrr.72
- Lambert JC, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tavernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fievet N, Barberger-Gateau P, Engelborghs S, De Deyn P, Mateo I, Franck A, Helisalmi S, Porcellini E, Hanon O; European Alzheimer's Disease Initiative Investigators, de Pancorbo MM, Lendon C, Dufouil C, Jaillard C, Leveillard T, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossu P, Piccardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanche H, Dartigues JF, Tzourio C, Gut I, Van Broeckhoven C, Alperovitch A, Lathrop M, Amouyel P. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nat Genet 2009;41:1094-9. https://doi.org/10.1038/ng.439
- Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schurmann B, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Hull M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet 2009;41:1088-93. https://doi.org/10.1038/ng.440
- Nuutinen T, Suuronen T, Kauppinen A, Salminen A. Clusterin: a forgotten player in Alzheimer's disease. Brain Res Rev 2009;61:89-104. https://doi.org/10.1016/j.brainresrev.2009.05.007
Cited by
- Profiles of Human Milk Oligosaccharides and Production of Some Human Milk Oligosaccharides in Transgenic Animals vol.3, pp.3, 2011, https://doi.org/10.3945/an.111.001529
- 구속 스트레스가 백서 타액선 조직 내의 clusterin 변화에 미치는 영향 vol.37, pp.2, 2011, https://doi.org/10.14476/jomp.2012.37.2.081
- Clusterin in neurological disorders: Molecular perspectives and clinical relevance vol.88, pp.5, 2011, https://doi.org/10.1016/j.brainresbull.2012.05.006
- 구속 스트레스에 대한 백서 타액선 조직의 미세구조적, 조직화학적 변화 vol.38, pp.2, 2011, https://doi.org/10.14476/jomp.2013.38.2.121
- A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin vol.37, pp.None, 2016, https://doi.org/10.1016/j.neurobiolaging.2015.09.009
- Identification of brain antigens recognized by autoantibodies in experimental autoimmune encephalomyelitis-induced animals treated with etomoxir or interferon-β vol.8, pp.None, 2018, https://doi.org/10.1038/s41598-018-25391-y
- Association between clusterin concentration and dementia: a systematic review and meta-analysis vol.34, pp.1, 2019, https://doi.org/10.1007/s11011-018-0325-0
- Clusterin enhances AKT2‐mediated motility of normal and cancer prostate cells through a PTEN and PHLPP1 circuit vol.234, pp.7, 2019, https://doi.org/10.1002/jcp.27768
- Increased clusterin levels after myocardial infarction is due to a defect in protein degradation systems activity vol.10, pp.8, 2019, https://doi.org/10.1038/s41419-019-1857-x
- Knockout of apolipoprotein A‐I decreases parenchymal and vascular β‐amyloid pathology in the Tg2576 mouse model of Alzheimer's disease vol.45, pp.7, 2011, https://doi.org/10.1111/nan.12556
- Clinical importance of serum secreted clusterin in predicting invasive breast cancer and treatment responses vol.12, pp.1, 2021, https://doi.org/10.1080/21655979.2020.1868732
- Clusterin: Always protecting. Synthesis, function and potential issues vol.134, pp.None, 2021, https://doi.org/10.1016/j.biopha.2020.111174